[go: up one dir, main page]

IE52611B1 - Recovering and concentrating nonferrous materials such as zinc and lead and apparatus therefor - Google Patents

Recovering and concentrating nonferrous materials such as zinc and lead and apparatus therefor

Info

Publication number
IE52611B1
IE52611B1 IE569/82A IE56982A IE52611B1 IE 52611 B1 IE52611 B1 IE 52611B1 IE 569/82 A IE569/82 A IE 569/82A IE 56982 A IE56982 A IE 56982A IE 52611 B1 IE52611 B1 IE 52611B1
Authority
IE
Ireland
Prior art keywords
reactor
zinc
lead
process according
combined form
Prior art date
Application number
IE569/82A
Other versions
IE820569L (en
Original Assignee
Samim Soc Azionaria Minero Met
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Samim Soc Azionaria Minero Met filed Critical Samim Soc Azionaria Minero Met
Publication of IE820569L publication Critical patent/IE820569L/en
Publication of IE52611B1 publication Critical patent/IE52611B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B19/00Obtaining zinc or zinc oxide
    • C22B19/34Obtaining zinc oxide
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B13/00Obtaining lead
    • C22B13/02Obtaining lead by dry processes
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B19/00Obtaining zinc or zinc oxide
    • C22B19/02Preliminary treatment of ores; Preliminary refining of zinc oxide

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Manufacturing & Machinery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

A process for recovering or concentrating Zn and Pb from primary or secondary raw materials, admixed with coal, the coal being partially burnt to produce CO, is carried out in two stages, during the first of which there is direct reduction of the material due to the effect of the coal and volatilization of zinc and of lead oxide, whereas in the second stage there is an oxidation in the vapour phase of the zinc produced in the first stage by the action of air and/or oxygen. An apparatus for carrying out the process is a reactor having a frustoconical outline and comprising a metal casing (2) internally lined with a refractory material (3) and rotated about its geometrically arranged vertical axis (1), the reactor being equipped with a bottom drain hole (5), for liquid material.

Description

This invention relates to a process for treating a particulate material containing zinc and lead each in combined form, for example in the form of oxides or sulphides of the metals. The materials used can be, for example, primary raw materials (ores) or secondary raw materials (such as steel work fumes, mineral residues and metallurgical slags).
The most important volatilization method used nowadays in order to recover or concentrate non-ferrous metals such as zinc and lead is the Waelz kiln method. In this method, the charge, which contains zinc (maximum 30% to 35%), lead, and other metals (to a lesser extent) is mixed with coke dust or anthracite dust in an amount of 18% to 25% by weight, and the mixture is charged into a conventional rotary kiln which is inclined by 2° to 4° relative to the horizontal.
Appreciable recovery of useful metals is thus obtained. The main shortcoming is the considerable bulk of the installation (due to the need to attain a very large exchange surface between the charge and atmospheric air) so that the sensible heat can be recovered only partially.
Another known process is the cyclone-oven process. In this process, the charge, mixed with coke dust, is put in a cylindrical cyclone oven wherein it is tangentially contacted by preheated air.
The fumigation is completed in an adjacent oven which is generally an electric-arc furnace. In the electric arc furnace, non-volatile material can be collected in a blank phase which is separate from the slag. Thus, there is a considerable consumption of energy. - 2 52611 Moreover, the charge must be completely dried and must have a particle size of one millimetre at the most.
It has now been surprisingly found that the drawbacks of the conventional methods can be overcome by using a single reaction zone having an environment which is partly oxidizing and partly reducing.
According to the present invention, there is provided a process for treating a particulate material containing zinc and lead each in combined form, which comprises (1) heating the material in the presence of a carbonaceous material so as to reduce the zinc in combined form to metallic zinc and so as to volatilize the metallic zinc, and so as to volatilize the lead in combined form as such or as lead oxide, or to reduce the lead in combined form to metallic lead, and (2) effecting oxidation of the zinc in the vapour phase in the presence of air and/or oxygen; the process being carried out in a rotating frustoconical reactor such that solid phase adheres to the wall of the reactor and such that liquid phase flows out of the reactor through a drain hole in the bottom of the reactor.
In the process of the invention, poor-grade coal and small sized coal can be used instead of natural gas or coke. These advantages do not offset the possibility of obtaining a satisfactory heat distribution pattern as well as the attainment of physico-chemical conditions which are suitable for the evolution of the reactions which are of interest.
In the process of the invention, there is used a mixture of material which contains lead and zinc in the form of their oxides or salts (such as sulphates, sulphides, silicates, aluminates and others) and a carbon-containing material. During the process, partial combustion of the carbon produces carbon monoxide.
The process comprises two stages. The first stage is a direct - 3 52611 reduction to form zinc from its oxides or salts, and volatilization of the zinc and of the lead oxide or salt contained in the starting material. The reduction takes place at the expense of the carbon contained in the carbonaceous material. The second stage is a vapour-phase oxidation of the zinc produced in the first stage, by the aid of a combustion supporter such as air and/or oxygen which is carried out concurrently with the zinc vapour formed.
The non-volatile content of the charge, which usually comprises CaO, SiOg and FeO, i.e. in an oxide state, and which contributes to form the slag, may have its concentrations of its various components so selected as to produce a slag at a melting point temperature not above 1200°C, so that non-volatiles may leave the reactor in the liquid phase. For this reason, it might be necessary to make appropriate additions to the starting materials if the concentrations of the components are not such as to fulfil the requirements specified hereinabove.
During the first stage, under determined and imposed conditions, metallic lead can be formed by the reaction: PbO + CO -> Pb (a liquid) + CO,.
* The metallic lead mixes with the slag but separates therefrom by gravity.
The carbon monoxide which is collected about the rotation axis entrains the volatilized products upwards and is burned with oxygen so that additional heat can be supplied to the process.
The process is preferably carried out at a temperature of from 1100 to 1600°C. - 4 52611 The process is carried out in a rotating frustoconical reactor such that solid phase adheres to the wall of the reactor and such that liquid phase flows out of the reactor through a drain hole in the bottom of the reactor. Thus, the process can be carried out in an apparatus as claimed in any claim of our Patent Application No &68/S2.
One apparatus suitable for performing the process is characterised in that it is frustoconical and consists of one or more frustoconical bodies possibly replaced by their respective internal or external enveloping surfaces, the reactor comprising a metal casing internally lined by refractory materials and being rotated about its vertically arranged geometrical axis, a drain hole being formed through the reactor bottom wall so that the solid charged materials, due to the effect of the various phases, adhere to the inner reactor walls and the liquid substances which are formed are allowed to run down towards the drain hole, the inside diameter of the larger end of the reactor being from 1 to 10 metres, the inside diameter of the smaller end of the reactor being from 0.2 to 1 metre, the diameter of the drain hole being from 5 to 100% of the inside diameter of the smaller end of the reactor, the angle of the generating line of the frustoconical body with the vertical being from 10° to 60°, and the rotational speed of the reactor being from 10 to 80 revolutions per minute. Preferably, in the case of a reactor consisting of more than one frustoconical body, the generating lines of the bodies do not have an inclination greater than 30° with respect to one another.
Reference will now be made, by way of example, to Figures 1 and 2 of the accompanying drawing, showing reactors suitable for use in - 5 11 the invention.
The reactor is frustoconical, and consists of one or more frustoconical bodies, possibly replaced by their external or internal enveloping surfaces. It is arranged so that its geometrical axis 1 is vertical. In use, the reactor is rotated about its axis 1. The reactor consists of a metal casing 2, internally lined with refractory bricks 3. The angular rotational speed and the angle 4 between the generating line of the inner surface of the wall of the or each frustoconical body (or its enveloping surface) and the vertical is such that the solid phase of the material heated in the reactor remains, from a dynamic standpoint, in equilibrium under the concurrent actions of the weight, the inertial rotational forces, and the frictional forces on the inner wall, whereas the liquid phase runs down towards the reactor base, which has a drain hole 5.
The inside diameter of the larger end of the reactor is from 1 to 10 metres, preferably from 2 to 6 metres, whereas the inside diameter of the small end of from 0.2 to 1 metre.
The diameter of the drain hole is from 5% to 30% of the inside diameter of the smaller end, up to even 100% of the inside diameter of the smaller end depending upon the potential output of the installation.
The angle of the generating line of the frustoconical body to the vertical is from 10° to 60°, angles greater than 20° being preferred. In the case of a reactor consisting of more than one frustoconical body or of an enveloped curved surface, the generating lines and their tangents preferably do not have an inclination greater than 30° with respect to one another. In use, the rotational speed of the reactor is usually from 10 to 80 rpm. - 6 52611 From two to four pipes or nozzles 6 and 7, with their ends opening into the inside of the inclined reactor, the nozzles being capable of being moved along a vertical axis, are used for charging both the feed material and the fuel. Alternatively, one or more pipes 8 (usually up to a maximum of four pipes) which are substantially parallel to the generating line of the inner surface, may be used. Through perforations 9 formed along the entire pipe length and possibly evenly spaced apart from each other, preheated air and/or oxygen is continuously blown into the reactor. This jet of combustion aid has a radial centrifugal component and a tangential component relative to the path at the point where the jet impinges on the reactor wall and along a direction concordant with the motion so as not to disturb the dynamic conditions of the charge which is held in the reactor, either in the liquid phase or the solid phase.
Lastly, there is a central pipe 10 for introducing a combustionaid, which is also used to burn the carbon monoxide formed and for bringing about oxidation of the zinc vapour.
The charge can be a primary raw material (an ore) and/or a secondary raw material (such as steelwork fumes, residual processing sludges and others) which contain lead and zinc in variable amounts such as from 1% and over. The particle size of the charge is usually from 0.01 to 5 mm.
The charge can be introduced in the upper section of the reactor after having been mixed with the fuel, the latter also being of fine particle size. Alternatively, the charge and fuel can be fed separately through the pipes 6 and 7 so as to obtain a sufficient heat evolution consistently with the desired temperatures, and also in order to provide a reducing environment in the upper section.
In the lower section of the oven, through one of the pipes which - 7 52611 is not otherwise used, the carbon-containing material is introduced to ensure the necessary thermal and processing (reducing) conditions.
The quantity of carbon used is a function of the quantity of zinc and is usually from 8% to 25% of the charge, preferably from % to 20% thereof.
As a combustion supporter, air, possibly preheated to 600°C and enriched with oxygen, or pure oxygen, possibly preheated to 200°C, are used.
The reaction velocity is very high by virtue of the considerably 10 large contact surface area between the individual phases, this being a direct consequence both of the fine particle size of the charge and fuel and the rotary motion of the reactor. The consumptions predicted are nearly stoichiometric.
An Example will now be given to illustrate the invention.
EXAMPLE The starting material is a steelwork fume containing 20% of zinc and 3.5% of lead. The reactor is a frustoconical vessel flared downwards, and comprises a sheet metal casing internally lined with a refractory sleeve. The diameter of the larger base of tbe cone (upper section) was 3800 mm, the diameter of the base of the lesser cone (lower section) was 800 mm, the height of the frustum of cone was 3000 mm, and the angles of the generating lines of the cone with respect to the vertical were 45° and 10°, respectively, for the upper and lower sections. The rotational speed of the cone was rpm, the oxygen flow rate was 5 normal cubic metres per minute, the feed rate for the cone was 4 kg per minute, and the feed rate of the charge was 65 kg per minute. The charge was admixed with 0.10 kg of coke per kg of charge, the coke being intended as auxiliary coke. - 8 52611 Under these conditions, one obtains an oxide containing 60S! of zinc and 10% of lead, with an output of 20 kg per minute and with yields of zinc and lead of the order of magnitude of 93% 95% and over.

Claims (9)

1. A process for treating a particulate material containing zinc and lead each in combined form, which comprises (1) heating the material in the presence of a carbonaceous material so as to reduce the zinc in combined form to metallic zinc and so as to volatilize the metallic zinc, and so as to volatilize the lead in combined form as such or as lead oxide, or to reduce the lead in combined form to metallic lead, and (2) effecting oxidation of the zinc in the vapour phase in the presence of air and/or oxygen; the process being carried out in a rotating frustoconical reactor such that solid phase adheres to the wall of the reactor and such that liquid phase flows out of the reactor through a drain hole in the bottom of the reactor.
2. A process according to claim 1, wherein the particulate material is heated to a temperature of from 1100 to 1600°C.
3. A process according to claim 1 or 2, wherein the particulate material has a particle size of from 0.01 to 5 mm.
4. A process according to any of claims 1 to 3, wherein the carbonaceous material is in particulate form.
5. A process according to claim 4, wherein the carbonaceous material has a particle size of from 0.01 to 5 mm.
6. A process according to any of claims 1 to 5, wherein the air and/or oxygen is preheated to a temperature of from 200 to 600°C.
7. A process according to any of claims 1 to 6, the process being carried out in an apparatus substantially as hereinbefore described with reference to Figure 1 or Figure 2 of the drawing. - 10 82611
8. A process for treating a particulate material containing zinc and lead each in combined form, substantially as described herein with reference to the Example.
9. The product of a process according to any of claims 1 to 8.
IE569/82A 1981-03-13 1982-03-12 Recovering and concentrating nonferrous materials such as zinc and lead and apparatus therefor IE52611B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT20343/81A IT1137505B (en) 1981-03-13 1981-03-13 PROCEDURE FOR THE RECOVERY OR CONCENTRATION OF NON-FERROUS MATERIALS SUCH AS ZINC AND LEAD AND EQUIPMENT TO CONDUCT THAT PROCEDURE

Publications (2)

Publication Number Publication Date
IE820569L IE820569L (en) 1982-09-13
IE52611B1 true IE52611B1 (en) 1987-12-23

Family

ID=11165882

Family Applications (1)

Application Number Title Priority Date Filing Date
IE569/82A IE52611B1 (en) 1981-03-13 1982-03-12 Recovering and concentrating nonferrous materials such as zinc and lead and apparatus therefor

Country Status (13)

Country Link
BE (1) BE892470A (en)
CS (1) CS235010B2 (en)
DE (1) DE3207026C2 (en)
DK (1) DK99782A (en)
FR (1) FR2501723A1 (en)
GB (1) GB2094772B (en)
GR (1) GR75875B (en)
IE (1) IE52611B1 (en)
IT (1) IT1137505B (en)
LU (1) LU83997A1 (en)
NL (1) NL8201028A (en)
SE (1) SE462978B (en)
YU (1) YU54482A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6682586B2 (en) * 2001-10-09 2004-01-27 Heritage Environmental Services, Llc. Assemblies and methods for processing zinc-bearing materials
DE602004006998T2 (en) * 2003-07-04 2008-05-15 Umicore RECOVERY OF NON-FERROUS METALS FROM ZINC RESIDUE
KR101145957B1 (en) 2003-09-29 2012-05-15 유미코르 Process and apparatus for recovery of non-ferrous metals from zinc residues
JP5473894B2 (en) 2007-03-19 2014-04-16 ユミコア ソシエテ アノニム Room temperature single phase Li insertion / extraction material for use in Li-based batteries
CN107881323B (en) * 2017-09-27 2019-07-16 昆明理工大学 Oxygen-enriched enhanced roasting method for non-ferrous metal mineral resources

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB290035A (en) * 1927-05-03 1928-05-10 Ernest Bury Process for the recovery of lead and zinc from zinc waste
FR1020527A (en) * 1950-06-19 1953-02-06 Process and plant for ore reduction
DE877957C (en) * 1951-07-26 1953-08-10 Metallgesellschaft Ag Process for blowing zinc-containing material
NL108800C (en) * 1954-05-28 1900-01-01
GB971729A (en) * 1962-08-20 1964-10-07 Imp Smelting Corp Ltd Improvements in the extraction of zinc
FR1375376A (en) * 1963-11-12 1964-10-16 Broken Hill Ass Smelter Method of treating metalliferous materials and apparatus used for this purpose
CA1033575A (en) * 1973-12-19 1978-06-27 John E. Allen Treatment of steel mill waste dusts containing zinc
DE2519810C2 (en) * 1975-05-03 1983-01-13 Fried. Krupp Gmbh, 4300 Essen Process for processing powdery material from metallurgical exhaust gases
DE2537626C3 (en) * 1975-08-23 1978-09-21 Duisburger Kupferhuette, 4100 Duisburg Process for improving the production of pure zinc oxide
DE2618630B2 (en) * 1976-04-28 1978-03-02 Enaf Empresa Nacional De Fundiciones, La Paz (Bolivien) Process for zinc extraction
FR2373612A1 (en) * 1976-12-13 1978-07-07 Siderurgie Fse Inst Rech PROCESS FOR EXTRACTING ZINC CONTAINED IN STEEL WASTE

Also Published As

Publication number Publication date
BE892470A (en) 1982-09-13
IE820569L (en) 1982-09-13
DE3207026C2 (en) 1985-10-10
FR2501723A1 (en) 1982-09-17
IT8120343A0 (en) 1981-03-13
GB2094772B (en) 1985-01-30
DE3207026A1 (en) 1982-09-16
DK99782A (en) 1982-09-14
LU83997A1 (en) 1983-02-22
GR75875B (en) 1984-08-02
GB2094772A (en) 1982-09-22
SE462978B (en) 1990-09-24
IT1137505B (en) 1986-09-10
NL8201028A (en) 1982-10-01
YU54482A (en) 1985-03-20
SE8201569L (en) 1982-09-14
CS235010B2 (en) 1985-04-16

Similar Documents

Publication Publication Date Title
JP3058039B2 (en) Converter steelmaking method
CA2636155C (en) Use of an induction furnace for the production of iron from ore
CA1244656A (en) Processes and appparatus for the smelting reduction of smeltable materials
US4006010A (en) Production of blister copper directly from dead roasted-copper-iron concentrates using a shallow bed reactor
JPS6227138B2 (en)
US3235374A (en) System and process for the direct reduction of iron ore
US4756748A (en) Processes for the smelting reduction of smeltable materials
CA2219415A1 (en) Process for recovering metals from iron oxide bearing masses
SU1128844A3 (en) Method of obtaining blister copper from copper ore
US2938782A (en) Method and operation of blast furnaces and metallurgical fuels therefor
US6136059A (en) Process for reducing the electric steelworks dusts and facility for implementing it
JPH05504375A (en) metal recovery
IE52611B1 (en) Recovering and concentrating nonferrous materials such as zinc and lead and apparatus therefor
CA1055553A (en) Extended arc furnace and process for melting particulate charge therein
CA1036830A (en) Autogenous smelting of lead in a top blown rotary converter
US5685244A (en) Gas-fired smelting apparatus and process
US3038795A (en) Process for smelting and reducing powdered or finely divided ores
US3471283A (en) Reduction of iron ore
JPS61104013A (en) Method for recovering iron contained in molten steel slag
US3542350A (en) Apparatus for continuous metal melting and refining
US3223521A (en) Methods for increasing the proportion of scrap metal charged to basic oxygen conversion processes
SU1740425A1 (en) Shaft plasma furnace for metal reduction
EP0216618A2 (en) Recovery of volatile metal values from metallurgical slags
GB2095220A (en) Concentrating antimony and tin
US4985067A (en) Process and device for implementing hot chemical processes